The human retinal pigment epithelium (RPE) is a potential target tissue for directed transfer of candidate genes to treat age-related macular degeneration (AMD). The RPE is uniquely suited to gene therapy protocols that use liposome-mediated DNA transfer because of its high intrinsic phagocytic func
CYTOKINE- AND NEUROPEPTIDE-MEDIATED DIFFERENTIATION IN RETINAL PIGMENT EPITHELIAL CELLSIN VITRO
β Scribed by HIROKO KISHI; HIROMU K. MISHIMA; UKI YAMASHITA
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 133 KB
- Volume
- 21
- Category
- Article
- ISSN
- 1065-6995
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β¦ Synopsis
To determine the mechanism of growth and differentiation of retinal pigment epithelial (RPE) cells it is important to understand the pathogenesis of several retinal diseases. Recently it has been reported that several cytokines and neuropeptides regulate the growth of RPE cells. In this study, the role of cytokines and neuropeptides in melanin synthesis, which is one indication of the RPE cell differentiation, was examined using chick RPE cells in vitro. IL-1 , TNF-, substance P, -endorphin and methionine-enkephalin stimulated the melanin synthesis of RPE cells in a dose-dependent manner. The most effective concentrations of these agents on RPE cell melanin synthesis were not the same as that for RPE cell proliferation. These results indicate that cytokines and neuropeptides play an important role not only for the growth but also for the differentiation of RPE cells.
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## Abstract Cultured monkey retinal pigment epithelial (RPE) cells rapidly secrete large amounts of insulinβlike growth factor binding proteins (IGFβBPs). IGFβII tracer binding activity in conditioned media is two to three times greater than that of IGFβI. Under reducing SDSβPAGE conditions, ^125^I